Disinfecting and antimicrobial compositions

ABSTRACT

Broad spectrum disinfecting and microbicidal compositions of biodegradable and environmentally friendly compositions containing esters formed from fatty organic alcohols and fatty carboxylic acids. These compositions display activities against the most resistant microbial forms including bacterial spores. The preparations can be used in health care, food processing, personal care and other industries where the use of harsh oxidizing chemicals is undesirable.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No.13/099,017filed May 2, 2011, now U.S. Pat. No. 8,574,609, which is acontinuation of U.S. application Ser. No. 11/337,163 filed Jan. 20,2006, which is a non-provisional of U.S. Provisional Patent App. Ser.No. 60/647,464 filed Jan. 28, 2005, the entire disclosures of which arehereby incorporated by reference.

BACKGROUND OF INVENTION

1. Field of Invention

This invention relates to cleaning compositions for body, food, and foodcontact surfaces which reduce the risk of illness caused by harmfulchemical residues, infectious agents and other disease causing andspoilage microbial agents. More particularly, the present inventionprovides chemical disinfecting compositions which reduce injury orinflammation to the skin. Even more particularly the present inventionconcerns disinfecting compositions which use safe and non-toxic chemicalagents selected from alcohol esters of ethyl lactate and its homologsfor preparing products with cleaning, solubilizing, antimicrobial andmicrobicidal properties.

2. Prior Art

Most common antimicrobial products such as chlorine, chlorine dioxideperacetic acid, ozone, hydrogen peroxide, UV- and other radiations, usedto reduce microbial population on food and other contact surfacespossess highly oxidizing and sometimes destructive properties. Theseoxidizing chemicals and physical agents inactivate microorganisms byreacting with their organic material. However, these chemicals alsoreact with organic food material and produce unknown chemical residuesoften harmful to human and animal health. Hypochlorite (chlorine)produces carcinogenic residues on food. These antimicrobial products donot have detergent action or cleaning properties. Some other cleaningpreparations that are allowed on food either do not have antimicrobialand microbicidal properties or are not safe enough as the ingredientsare not considered by the FDA as GRAS or food additive safe. Some otherpreparations have disinfecting properties without the solubilizingproperties to remove harmful pesticide residues. Still some othercleaning products need to incorporate antibacterial compounds in thesepreparations to inhibit or kill microorganisms.

Thus, there is a need for cleaning compositions containing antimicrobialand disinfecting properties which do not exhibit the deleteriousproperties identified above.

The antimicrobial cleaning compositions of this invention, as describedbelow, employ all GRAS and/or food grade additive ingredients withcleaning, solubilizing, detergent and antimicrobial properties.

SUMMARY OF INVENTION

In accordance herewith, there is provided a class of chemicalcompositions predicated on chemical agents that can be used to prepareantimicrobial, microbicidal and disinfecting compositions for cleaningfresh fruits, vegetables, seeds, sprouts, meats, poultry, eggs,carcasses, other food surfaces and surgical instruments as well as bodyparts in order to prevent, to reduce or to eliminate the risk ofinfection and illness arising from both chemical residues andmicroorganisms spread by or carried on the food, food contact and bodysurfaces.

The antimicrobial cleaning and disinfecting composition hereofcomprises:

(a) at least one alcohol ester of an organic acid, alone, or inadmixture with one or more of,

(1) an antimicrobial surface active agent selected from chemicalsclassified as GRAS or food grade additive by the US FDA;

(2) an emulsifying surface active agents classified as GRAS or foodgrade additive by the USFDA;

(3) an organic acidifying agent selected from chemicals classified asGRAS or food grade additive by the USFDA which adjust the pH of thecomposition between 2 to 12;

(4) a chelant, either organic or inorganic, selected from chemicalsclassified as GRAS or food grade additive by the USFDA;

(5) a reducing agent or an antioxidant selected from chemicalsclassified as GRAS or food grade additive by the USFDA, and

(6) a diluent to dissolve, disperse or suspend the ester and any one ofthe above ingredients.

The composition hereof may include other compatible ingredients, whichdo not reduce or interfere with the antimicrobial and cleaningproperties such as for example, urea, to enhance the cleaning propertiesof the composition.

The composition may, additionally, include a coloring agent, fragrances,vitamins, nutritive agents and/or a thixotropic agent or other agents,which alter physical and functional properties of the composition as,desired.

The present cleaning compositions can be prepared in either concentratedliquid or powder forms as well as in gel form, or as in a foam, thus,giving operational flexibility for use. The concentrate can be furtherdiluted to form a use composition.

For a more complete understanding of the present invention reference ismade to the following detailed description and accompanying illustrativeexamples.

DESCRIPTION OF THE PREFERRED EMBODIMENT

As noted hereinabove, the present invention provides a cleaning anddisinfecting compound using GRAS or food grade additives and whichcomprises an alcohol ester of an organic acid used alone or in admixturewith any one of: (a) surface active agents, (b) emulsifying agents, (c)acidifying agents, (d) sequestrants or chelants, (e) reducing agents orantioxidants, and/or (f) a diluent.

Other adjuvants such as fragrances, coloring agents and the like may,also be incorporated into the composition.

With more particularity, the alcohol ester contemplated for use hereinis the reaction product of a C to C.sub.12 fatty alcohol and a C.sub.1to C.sub.8 fatty acid.

The ester hereof may be represented by the formula:R—COO—R.sub.1

-   -   where R is an acid moiety and is either C.sub.nH.sub.2n+1 or        C.sub.nH.sub.2n+1O    -   where n is an integer ranging from about 1 to about 8 and        R.sub.1 is an alcohol moiety corresponding to the formula        C.sub.mH.sub.m+1 here m is an integer ranging from about 1 to        about 12.

Respective useful esters include, for example, methyl lactate, ethyllactate, propyl lactate, butyl lactate, etc., and the like, as well asmixtures thereof.

Among the surface active agents classified by the US FDA as generallyregarded as safe (GRAS) and or classified as food additive, and havingantimicrobial properties that impart additional cleaning microbicidalproperties that may be incorporated into the composition hereof,include, for example lactylic esters of C.sub.6 to C.sub.16 fatty acidand the corresponding alkali salts. Other useful compounds include, forexample, dioctyl sodium sulfosuccinate, sodium lauryl sulfate, salts offatty acids and sodium mono and dimethyl naphthalene sulfonate. Mixturesof such surfactants may be used herein.

Representative of useful emulsifying agents include, for example, foodgrade or GRAS lecithin, polysorbate 60, polysorbate 65, polysorbate 80,sucrose fatty acid esters, salts of stearyol 2-lactylate and the like,as well as mixtures thereof.

The acidifying agent, where used, may be selected from acetic acid,adipic acid, ascorbic acid, benzoic acid, citric acid, dehydroaceticacid, erythorbic acid, fumaric acid, glutaric acid, gluconic acid,hyaluronic acid, hydroxyacetic acid, lactic acid, malic acid, sorbicacid, succinic acid, tannic acid, tartaric acid, sulfuric acid,phosphoric acid, nitric acid, hydrochloric acid, sulfamic acid,carboxylic acid polymers, homo- or hetero-polymerized carboxylic acidsuch as poly lactic acid or poly lactic-glycollic acid, and the like, aswell as mixtures thereof Where used, the acidifying agent is,preferably, lactic acid.

Either an organic or inorganic sequestrating or chelating agent selectedfrom chemicals classified as GRAS or food grade additive by the US FDAsuch as gluconic acid and citric acid esters such as isopropyl citrate,monoisopropyl citrate, and stearyl citrate may, also, be used herein.

Also, a reducing agent or an antioxidant selected from chemicalsclassified as GRAS or food additive by the US FDA such as BHT, propylgallate, and L-cysteine, and the like, may be used herein.

The composition may be admixed with a suitable diluent be it liquid,powder, gel or foam form to dissolve or disperse or suspend thecomponent(s). The dilutent is selected from chemicals classified as GRASor food additive by the US FDA, and include, for example, ethyl alcohol,propylene glycol, isopropyl alcohol, water, fatty acid esters ofcarbohydrates including sucrose, sorbitol and the like, other usefuldiluents include, for example, triglycerides of fatty acids, derivativesor simple compounds of silica, cellulose, starch and natural products orsynthetic polymers, and the like, as well as mixtures thereof Preferreddiluents include water, ethanol as well as propylene glycol and mixturesthereof

Where the composition is the ester itself it is dispersed in a suitablediluent to form a concentrate containing from about 0.001% to about99.999%, by weight, of the ester and, preferably, from about 0.01% toabout 99.999%, by weight, of ester.

Where the ester is used in conjunction with any of the aforementionedadditional components, generally, the ester will be present in thecomposition, in an amount ranging from about 0.001% to about 99.99%, byweight, based on the total weight of the concentrate.

Generally, where the additional component is a surface active agent, theconcentrate will contain from about 0.01% to about 40.00%, by weight, ofthe surfactant based on the weight of the concentrate.

Where the ester is used with an emulsifier, the concentrate willcomprise from about 0.01% to about 40.00% by weight of the emulsifierbased on the weight of the concentrate.

Where the adjuvant is an acidifying agent, it will be present in anamount ranging from about 0.01% to about 40% by weight of the acidifyingagent based on the weight of the acidifying concentration.

The chelant, where used, will be present in the concentrate in an amountranging from about 0.01% to about 10% by weight, based upon the totalweight of the concentrate.

With respect to the reducing agent or antioxidant, where used, informing the concentrate it will be present in an amount ranging fromabout 0.01% to about 40.00% by weight, based on the weight of theconcentrate.

Where the concentrate is an admixture of each of the adjuvants, theresulting composition will contain from about 0.01% to about 99.99%, byweight, of the ester; from about 0.01% to about 40.00% by weight, of thesurfactant; from about 0.01% to about 40.00% by weight, of theemulsifier; from about 0.01% to about 10.00% by weight, of the chelant;from about 0.01% to about 40.00% by weight, of the reducing agent, allbased upon the total weight of the concentrate.

In preparing the concentrate, it is prepared at room temperature, byadmixing the components together.

In forming the use solution, the use solution will contain from about0.01% to about 99.99% by weight, of the ester and from about 0.01% toabout 99.99% by weight, of the additional component, be it any onecomponent or a mixture thereof.

The use solution is prepared at room temperature by mixing or admixingtogether the concentrate with the diluent.

Where the diluent is a powder, the powder is brought into a solution orsuspension with the concentrate, the powder being mixed therewithin.

Generally, the final form of the use composition will contain from about0.01% to about 99.99%, by weight, of ester; from about 0% to about99.99%, by weight of adjuvant or additional component and from about0.01% to about 99.99%, by weight, based on the final form of the usecomposition of diluent.

The composition hereof is storage stable and exhibits antimicrobialcleaning and disinfecting properties.

For a more complete understanding of the present invention, reference ismade to the following examples, which are to be constructed asillustrative not limitations of the present invention, all parts are byvolume.

EXAMPLE I

This example illustrates the sporicidal activity of lactic estersagainst Bacillus coagulans spores.

One ml each of a mixture of ethyl lactate and butyl lactate (1:1) wasmixed, at room temperature, with 0.1 ml of B. coagulans spore suspensioncontaining 1.5.times.10.sup.6 spores per ml and incubated at roomtemperature for five minutes. B. coagulans exhibit very high heatresistance and is used as an indicator for bacteria in a heatsterilization process.

After five minutes 1 ml of the test mixture was mixed with 10 mls ofButterfield's buffer, at pH 7.0. Then, 0.1 ml of the buffered testmixture was plated on a plate count in agar. The colonies were countedafter 48 hrs of incubation at room temperature.

The following table, Table I, shows the results of the colony counting.

TABLE 1 Sporicidal Activity of Lactic Esters Starting Number of Sporesin the inoculum: 1.5 × 10⁶/ml Number of spores in the test (diluted1:10): 1.5 × 10⁵/ml Number of spores in the buffer (diluted 1:11): 1.4 ×10⁴/ml Number of spores plated (0.1 ml): 1.4 × 10³/ml Surviving numbercolony forming units: 150/plate Percentage killed (1.4 × 10³ − 150) ×100: 89.28%

Example 1 shows that the mixture of ethyl lactate and butyl lactatedisplays sporicidal activity.

EXAMPLE II

This example illustrates the microbicidal activity of ethyl lactate andbutyl lactate against vegetative bacteria. Example II, also, shows theminimum lethal activity (MLC) of these lactic esters against both grampositive and gram-negative bacteria.

The microbicidal activity was further investigated by determining theminimum inhibitory concentration (MIC) and minimum lethal concentrations(MLC) of these esters.

The tests were carried out in 10 ml of brain heart infusion broth. Theesters were serially diluted in brain heart infusion broth of samplesof, 0.1, 0.2, 0.3, 0.4 and 0.5/10 ml and challenged with 0.1 ml of 1/100dilution of 24 hr old brain heart infusion bacterial culture. The lowestconcentration determined the minimum inhibitory concentration (MIC). Thesamples were observed after 48 hrs at 37.degree. C. A loopful from tubeswithout growth were plated on BHI agar plates and observed for growthfor 24 to 48 hrs at 37.degree. C. The samples with the lowestconcentration of the ester without bacterial growth on the platesrepresented the minimum lethal concentration (MLC).

Tables 2 and 3, below, show the results of the tests.

TABLE 2 Antimicrobial Properties of Ethyl Lactate Concentration of Ethyllactate Test Organism 0.5% 1% 2% 3% 4% 5% E. coli 0157;H7 MLC + + − − −− MLC + + + − − − Listeria monocytogenes MLC + + + + + + MLC + + + + + +Pseudomonas aeruginosa MLC + + − − − − MLC + + + + − − Staphylococcusaureus MLC + + + + + − MLC + + + + + + Salmonella typhimuriumMLC + + + + − − MLC + + + + + + MIC = Minimum Inhibitory Concentration,MLC = Minimum Lethal Concentration; + = growth (inactive); − = no growth(active)

TABLE 3 Antimicrobial Properties (MLC) of Butyl Lactate Concentration ofButyl lactate Test Organism 0.5% 1% 2% 3% 4% 5% Pseudomonas aeruginosaMLC + + + − − − Listeria monocytogenes MLC + + − − − − MIC = MinimumInhibitory Concentration, MLC = Minimum Lethal Concentration; + = growth(inactive); − = no growth (active)

EXAMPLE III

This example illustrates the enhancement of antimicrobial activity oflactic esters by the incorporation of additional components therewith.

A series of samples of (a) methyl lactate, (b) ethyl lactate and (c)butyl lactate, alone, and in admixture with varying amounts of decyllactate and sodium dodecyl sulfates were used to test minimum inhibitoryactivity (MIC) by the method described in Example II, against thecultures of E. coli 0157 H7, Listeria monocytogenes, Staphylococcusaureus, Salmonella typhi, and Pseudomonas aeruginosa. Tables 4 and 5show that decyl lactate and sodium dodecyl sulfate enhanced inhibitoryactivities against the test bacteria.

TABLE 4 Enhancement of Antimicrobial Properties (MIC) of Ethyl lactateby Decyl lactylate Test Organism Test Compound 1% 2% 3% 4% 5% E. coli0157;H7 EL + + + − − EL + DL + + − − − Listeria monocytogenesEL + + + + + EL + DL − − − − Staphylococcus aureus EL + + + + + EL + DL− − − − − Salmonella typhi EL + + + − − EL + DL + + − − MIC = MinimumInhibitory Concentration, + = growth (inactive); − = no growth (active)

-   -   In undiluted form these esters were found to kill all vegetative        bacteria on contact.

TABLE 5 Enhancement of Antimicrobial Properties (MIC) of Lactic estersby Sodium dodecyl sulfate against Pseudomonas aeruginosa SDSConcentration of Lactic Esters Test Organism DL ppm 0.5% 1% 2% 3% 4% 5%Methyl lactate MIC 0.0 + + − − − − 50 − − − − − − 100 − − − − − − 200 −− − − − − Ethyl lactate MIC 0.0 + + − − − − 50 − − − − − − 100 − − − − −− 200 − − − − − − Butyl lactate MIC 0.0 + + − − − − 50 − − − − − − 100 −− − − − − 200 − − − − − − MIC = Minimum Inhibitory Concentration, MLC =Minimum Lethal Concentration; + = growth (inactive); − = no growth(active)

These results show that the microbicidal activity of lactic esters canbe enhanced to include a broad spectrum activity against both bacterialspores as well as vegetative bacterial pathogens.

EXAMPLE IV

This example illustrates the MIC and MLC of esters of lactic acidagainst yeast: Saccaromyces cerevisiae.

A 0.1 ml of 1/100 dilution of 48 hr old culture of S. cerevisiae wasused as inoculum. The test was performed using Sab. broth. The tubeswere incubated at room temperature 25.degree. C. The test was read after48 hrs. The results are shown in Tables 6 and 7 below.

TABLE 6 Antimicrobial activity against Saccharomyces cerevisiaeInhibitory (MIC)/Lethal (MLC) Test Concentration Test Ester Type 1% 1.5%2% 3% 4% Methyl lactate MIC + + + − − MLC + + + − − Ethyl lactate MIC +− − − − MLC + + − − − Butyl lactate MIC − − − − − MLC − − − − −

TABLE 7 Enhancement of Antimicrobial Properties (MIC) of Lactic estersby Sodium dodecyl sulfate against saccharomyces cerevisiae Inhibitory(MIC)/Lethal (MLC) Sodium lauryl Concentration Ester Tested sulfate(ppm) 1% 1.5% 2% 3% 4% Methyl lactate 200 MIC + + + − − MLC + + + − −Ethyl lactate 200 MIC + − − − − MLC + + − − − Butyl lactate 200 MIC − −− − − MLC − − − − −

EXAMPLE V

This example shows that ethyl lactate can be used to solubilize otherantimicrobial agents or ingredients that have low solubility in aqueoussolutions. In this example ethyl lactate was used to prepare aqueousantifungal preparations of dehydroacetic acid.

Into a suitable reaction vessel dehydroacetic was mixed together at roomtemperature 5.0 parts of dehydroacetic acid in 100 ml of ethyl lactate.

A clear solution was formed. A 0.1 ml sample was added to 2 ml of a waxcoating sample. The mixture was homogeneous and did not showprecipitate. The final concentration of dehydroacetic acid in thecoating solution was 2,500 ppm. Thus, imparting antifungal properties towax coating.

By reducing the spoilage microbial population the present esters, alone,or in combination with any of the above additives helps to increase theshelf life and/or keeping qualities of food. Thus the invention offersto prevent economic loss due to food spoilage and improves public healthand curtails medical costs arising from food-borne and other infectiousagents.

The alcohol esters of fatty acids hereof also display lethal activityagainst difficult to kill bacterial spores. These microbicidal agentscan also be incorporated into household, personal care, health care andhomeland security-related products. By incorporating other non-toxic,and generally regarded as safe (GRAS) or other ingredients considered asfood additive by the United States Food and Drug Administration (USFDA), the technology provides the potential to replace products withtoxic manifestation. In addition to microbicidal properties these agentscan be used to solubilize and to remove certain water insoluble harmfulresidues from food.

The compositions can also be used to clean and disinfect inanimatesurfaces. The composition can also be used to prepare personal care andhealthcare products used for preventing and reducing skin infections,either by direct application or by incorporating in ointments, bandagesor other carriers. Further the chemicals can also be used to destroyharmful bacterial spores that are very resistant to known disinfectingagents.

These esters can also be formulated with other ingredients to preparehighly effective microbicidal products for cosmetic personal care,healthcare, pharmaceutical and other industries. Powerful microbicidaland cleaning products can be developed incorporating these esters inproduct formulations.

Having thus described the invention, what is claimed is:
 1. A method ofcleaning a surface comprising: preparing a disinfecting composition thatconsists of an ester selected from the group consisting of methyllactate, ethyl lactate, butyl lactate, propyl lactate, hexyl lactate,octyl lactate, and mixtures thereof, wherein the disinfectingcomposition is food additive safe; and applying the composition to asurface containing microbes, bacteria, and bacterial spores to therebytreat the surface to clean the surface and to reduce the microbial countand wherein the composition has sporicidal activity effective to kill atleast 89% of the bacterial spores on the surface.
 2. The method as setforth in claim 1, wherein the disinfecting composition consists of amixture of ethyl lactate and butyl lactate.
 3. The method as set forthin claim 1 wherein the surface is the surface of a fruit or vegetable.4. The method as set forth in claim 1 wherein the surface is human skin.